2020
DOI: 10.4103/japtr.japtr_31_20
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Antioxidant and cytotoxic activities of the ethyl acetate extract of Sphagneticola trilobata (L.) J.F. Pruski on MCF-7 breast cancer cell

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Cited by 10 publications
(9 citation statements)
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“…[12] reported that secondary metabolites of flavonoids and steroids have the potential to prevent and treat cancer with high cytotoxic activity using the Brine Shrimp Lethality Test (BSLT) method. Sphagneticola trilobata contains metabolite compounds such as flavonoids and steroids that have the potential to prevent and treat cancer [6]. The role of plant compounds as prevention and repair by preventing karsinogens from reaching the target location (initiation), inhibiting malignant transformation of cells during the promotion or progression phase so that the growth of proliferating cells is not controlled so that cancer cells will be inhibited from metastasizing.…”
Section: Resultsmentioning
confidence: 99%
“…[12] reported that secondary metabolites of flavonoids and steroids have the potential to prevent and treat cancer with high cytotoxic activity using the Brine Shrimp Lethality Test (BSLT) method. Sphagneticola trilobata contains metabolite compounds such as flavonoids and steroids that have the potential to prevent and treat cancer [6]. The role of plant compounds as prevention and repair by preventing karsinogens from reaching the target location (initiation), inhibiting malignant transformation of cells during the promotion or progression phase so that the growth of proliferating cells is not controlled so that cancer cells will be inhibited from metastasizing.…”
Section: Resultsmentioning
confidence: 99%
“…The methanolic extract was then phytochemically screened for the presence of flavonoids, alkaloids, saponins, steroids, tannins, and phenols employing the procedures used in our previous report. [ 6 ]…”
Section: Methodsmentioning
confidence: 99%
“…The antioxidant activity was quantitatively analysis in vitro carried out using 2,2-diphenyl-1-picrylhydrazyl (DPPH) method (in triplicate) as previously described. [ 6 15 ] The extract solution with different concentrations (25–200 μg/mL) was prepared by dissolving the extract using mL methanol p.a. As much as 4 mL dissolved extract was then mixed with 1 mL (0.4 mM), followed by 30 min incubation in a dark condition at 37°C and measured using ultraviolet-visible spectrophotometer (Infinite M200, Tecan, Switzerland) at'.…”
Section: Methodsmentioning
confidence: 99%
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